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The Ulster Medical Journal|October 2, 2013
Outcome of 131I therapy in hyperthyroidism using a 550MBq fixed dose regimenAnthony Lewis, Brew Atkinson, Patrick Bell, et al.Pediatric Cardiology|June 26, 2026
Incidence, Genetic Characteristics, and Outcomes of Paediatric Cardiomyopathy in a National Cohort (2003-2025)Scott Kendall, Shannon Scott, Peter McClung, et al.Sleep|March 26, 2021
Late-in-life neurodegeneration after chronic sleep loss in young adult miceJessica E Owen, Yan Zhu, Polina Fenik, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 17, 2018
Chronic Sleep Disruption Advances the Temporal Progression of Tauopathy in P301S Mutant MiceYan Zhu, Guanxia Zhan, Polina Fenik, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|July 29, 2010
Heart Rhythm UK position statement on clinical indications for implantable cardioverter defibrillators in adult patients with familial sudden cardiac death syndromesClifford J Garratt, Perry Elliott, Elijah Behr, et al.Journal of Analytical Toxicology|April 5, 2017
Urinary Concentrations of Topically Administered Pain MedicationsMichele A Glinn, Andrew J Lickteig, Luke Weber, et al.The Journal of Clinical Investigation|May 3, 2008
The E1784K mutation in SCN5A is associated with mixed clinical phenotype of type 3 long QT syndromeNaomasa Makita, Elijah Behr, Wataru Shimizu, et al.European Journal of Pediatrics|March 3, 2026
Physical activity and competitive sport safety for children affected by inherited cardiac conditions and selected acquired cardiomyopathies: emerging evidence and areas for further inquiryScott Kendall, Andrea Greco, Nicoletta Cantarutti, et al.Scientific Data|September 3, 2024
Effects of changing farming practices in African agricultureTodd S Rosenstock, Peter Steward, Namita Joshi, et al.Nature Genetics|February 10, 2009
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants, Sekar Kathiresan, Benjamin F Voight, et al.Pageof 2